Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jill M. O'Reilly"'
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 61:73-77
The JAr choriocarcinoma cell cultures have demonstrated high levels of aromatase activity and have been useful for assaying a wide variety of aromatase inhibitors for aromatase inhibition in intact cells. Recently, several 7alpha-arylaliphatic androg
Autor:
Michael V. Darby, Anne L. Quinn, Carl J. Lovely, Xin Ju Gu, David C. Baker, Jill M. O'Reilly, Nancy E. Gilbert, Patrick J Ward, Robert W. Brueggemeier
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 61:247-254
The inhibition of aromatase, the enzyme responsible for converting androgens to estrogens, is therapeutically useful for the endocrine treatment of hormone-dependent breast cancer. Research by our laboratory has focused on developing competitive and
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 59:93-102
Inhibition of aromatase, the enzyme responsible for converting androgens to estrogens, may be therapeutically useful for the endocrine treatment of hormone-dependent breast cancer. Previous research on 7alpha-thiosubstituted androgens, especially 7al
Publikováno v:
Current Medicinal Chemistry. 3:11-22
Abstract: Aromatase (estrogen synthase) is an enzyme complex responsible for the conversion of androgens to estrogens in the final step in steroidogenesis. Estrogens play important roles in both normal physiology and reproduction and in certain estro
Publikováno v:
ChemInform. 26
Publikováno v:
Journal of medicinal chemistry. 38(15)
The inhibition of aromatase, the cytochrome P450 enzyme complex responsible for the conversion of androgens to estrogens, may be useful for the endocrine treatment of breast cancer. Previously, several 7 alpha-thio-substituted androstenediones have b